{{Rsnum
|rsid=104894625
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PMP22
|position=15260663
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PMP22
}}{{omim
|id=601097
|rsnum=104894625
|variant=0019
}}{{ClinVar
|rsid=104894625
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=15163980
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=PMP22:5376
|GENE_NAME=PMP22
|GENE_ID=5376
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.15163980G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1205; 601097.0019
|CLNSIG=5
|CLNCUI=C0393814; C1861674
|CLNDBN=Hereditary liability to pressure palsies; Charcot-Marie-Tooth disease, type IA
|Disease=Hereditary liability to pressure palsies; Charcot-Marie-Tooth disease
|CLNACC=RCV000008958.1; RCV000008959.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1392:C0393814:162500:640:230558006; NBK1205:C0270911:118220:101081:40632002
}}